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Home / Blog - Page 70

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U.S. FDA approved expanded indication of Gilead’s Biktarvy for Treatment of HIV-1 in pediatric populations
Biotechnology | FDA | HIV | Therapeutics

U.S. FDA approved expanded indication of Gilead’s Biktarvy for Treatment of HIV-1 in pediatric populations

On Oct. 18, 2021, Gilead Sciences announced that the Food and Drug Administration had approved a new low-dose…

Read More U.S. FDA approved expanded indication of Gilead’s Biktarvy for Treatment of HIV-1 in pediatric populationsContinue

LogicBio Therapeutics announced early clinical trial results demonstrated first-ever in vivo genome editing in children
Genomics | Life Science History

LogicBio Therapeutics announced early clinical trial results demonstrated first-ever in vivo genome editing in children

On Oct. 18, 2021, LogicBio Therapeutics announced clinical trial results that demonstrated the first-ever in vivo genome editing…

Read More LogicBio Therapeutics announced early clinical trial results demonstrated first-ever in vivo genome editing in childrenContinue

Athenex and Center for Cell and Gene Therapy announced allowance of first U.S. patent around CAR-NKT cell therapy
Biotechnology | Non-Profit Research | Therapeutics

Athenex and Center for Cell and Gene Therapy announced allowance of first U.S. patent around CAR-NKT cell therapy

On Oct. 18, 2021, Athenex and the Center for Cell and Gene Therapy at Baylor College of Medicine,…

Read More Athenex and Center for Cell and Gene Therapy announced allowance of first U.S. patent around CAR-NKT cell therapyContinue

Pfizer and BioNTech submitted data to EMA for vaccination of children 5 to <12 years of age with COMIRNATY
Biotechnology | COVID-19 | Pharmaceutical | Therapeutics | Vaccine

Pfizer and BioNTech submitted data to EMA for vaccination of children 5 to <12 years of age with COMIRNATY

On Oct. 18, 2021, Pfizer and BioNTech announced that the European Medicines Agency’s Committee for Human Medicinal Products…

Read More Pfizer and BioNTech submitted data to EMA for vaccination of children 5 to <12 years of age with COMIRNATYContinue

FDA approved naloxone injection to counteract opioid overdoses
FDA | Life Science History

FDA approved naloxone injection to counteract opioid overdoses

On Oct. 18, 2021, the Food and Drug Administration approved ZIMHI (naloxone hydrochloride) injection as an additional option…

Read More FDA approved naloxone injection to counteract opioid overdosesContinue

Relief’s collaboration partner published positive aviptadil data in high comorbidity critical COVID-19 patients
COVID-19 | Life Science History

Relief’s collaboration partner published positive aviptadil data in high comorbidity critical COVID-19 patients

On Oct. 15, 2021, RELIEF THERAPEUTICS reported that the parent company of its U.S. collaboration partner, NRx Pharmaceuticals,…

Read More Relief’s collaboration partner published positive aviptadil data in high comorbidity critical COVID-19 patientsContinue

Merck received positive CHMP opinion for VAXNEUVANCEル (Pneumococcal 15-valent conjugate vaccine)
Life Science History

Merck received positive CHMP opinion for VAXNEUVANCEル (Pneumococcal 15-valent conjugate vaccine)

On Oct. 15, 2021, Merck announced that the European Medicines Agencyメs Committee for Medicinal Products for Human Use…

Read More Merck received positive CHMP opinion for VAXNEUVANCEル (Pneumococcal 15-valent conjugate vaccine)Continue

FDA approved Roche’s Tecentriq as adjuvant treatment for certain people with early non-small cell lung cancer
Biotechnology | Diagnostics | Disease | FDA | Oncology | Radiology | Therapeutics

FDA approved Roche’s Tecentriq as adjuvant treatment for certain people with early non-small cell lung cancer

On Oct. 15, 2021, Roche announced that the U.S. Food and Drug Administration (FDA) had approved Tecentriq (atezolizumab)…

Read More FDA approved Roche’s Tecentriq as adjuvant treatment for certain people with early non-small cell lung cancerContinue

Pfizer and BioNTech submitted data to EMA for vaccination of children 5 to <12 years of age with COMIRNATY
Biotechnology | COVID-19 | Pharmaceutical | Therapeutics | Vaccine

Pfizer and BioNTech submitted data to EMA for vaccination of children 5 to <12 years of age with COMIRNATY

On Oct. 15, 2021, Pfizer and BioNTech announced they had submitted data supporting the vaccination of children 5…

Read More Pfizer and BioNTech submitted data to EMA for vaccination of children 5 to <12 years of age with COMIRNATYContinue

USDA confirmed COVID-19 infection in a Coatimundi at an Illinois Zoo
Agriculture | COVID-19 | Life Science History

USDA confirmed COVID-19 infection in a Coatimundi at an Illinois Zoo

On Oct. 14, 2021, the U.S. Department of Agriculture’s Agriculture Research Service (ARS) announced confirmation of SARS-CoV-2 (the…

Read More USDA confirmed COVID-19 infection in a Coatimundi at an Illinois ZooContinue

NIH RADx initiative expanded COVID-19 testing innovation for additional types of rapid tests
COVID-19 | Life Science History | NIH

NIH RADx initiative expanded COVID-19 testing innovation for additional types of rapid tests

On Oct. 14, 2021, The NIH Rapid Acceleration of Diagnostics (RADx) initiative announced that it has issued contract…

Read More NIH RADx initiative expanded COVID-19 testing innovation for additional types of rapid testsContinue

Moderna announced FDA Advisory Committee unanimously voted in support of EUA for booster dose of COVID-19 vaccine
Biotechnology | COVID-19 | FDA | Infectious Disease | Vaccine

Moderna announced FDA Advisory Committee unanimously voted in support of EUA for booster dose of COVID-19 vaccine

On Oct. 14, 2021, Moderna confirmed that the U.S. Food and Drug Administration’s (FDA) Vaccines and Related Biological…

Read More Moderna announced FDA Advisory Committee unanimously voted in support of EUA for booster dose of COVID-19 vaccineContinue

FDA accepted REGEN-COVᆴ (casirivimab and imdevimab) for priority review for treatment and prophylaxis of COVID-19
COVID-19 | FDA | Life Science History

FDA accepted REGEN-COVᆴ (casirivimab and imdevimab) for priority review for treatment and prophylaxis of COVID-19

On Oct. 14, 2021, Regeneron announced that the U.S. Food and Drug Administration (FDA) had accepted for priority…

Read More FDA accepted REGEN-COVᆴ (casirivimab and imdevimab) for priority review for treatment and prophylaxis of COVID-19Continue

Tuberculosis deaths rose for the first time in more than a decade due to the COVID-19 pandemic
COVID-19 | Life Science History

Tuberculosis deaths rose for the first time in more than a decade due to the COVID-19 pandemic

On Oct. 14, 2021, the World Health Organization announced that the COVID-19 pandemic had reversed years of global…

Read More Tuberculosis deaths rose for the first time in more than a decade due to the COVID-19 pandemicContinue

Cepheid received CE Mark for Xpert Xpress CoV-2/Flu/RSV plus
COVID-19 | Life Science History

Cepheid received CE Mark for Xpert Xpress CoV-2/Flu/RSV plus

On Oct. 14, 2021, Cepheid announced it had received the CE mark for Xpert Xpress CoV-2/Flu/RSV plus, a…

Read More Cepheid received CE Mark for Xpert Xpress CoV-2/Flu/RSV plusContinue

Democratic Republic of the Congo started Ebola vaccination
Life Science History

Democratic Republic of the Congo started Ebola vaccination

On Oct. 13, 2021, the Ministry of Health of the Democratic Republic of the Congo announced that vaccination…

Read More Democratic Republic of the Congo started Ebola vaccinationContinue

WHO bestowed posthumous award on the late Henrietta Lacks
Biotechnology | COVID-19 | HIV | Life Science History | Non-Profit Research | Polio | Therapeutics | Vaccine | WHO

WHO bestowed posthumous award on the late Henrietta Lacks

On Oct. 13, 2021, the World Health Organization (WHO) honoured the late Henrietta Lacks with a WHO Director-General’s…

Read More WHO bestowed posthumous award on the late Henrietta LacksContinue

Lucira’s Health COVID-19 test approved for sale in Singapore
Biotechnology | COVID-19

Lucira’s Health COVID-19 test approved for sale in Singapore

On Oct. 12, 2021, Lucira Health announced that it had received PSAR approval for its Lucra CHECK IT…

Read More Lucira’s Health COVID-19 test approved for sale in SingaporeContinue

CureVac shifted focus of COVID-19 vaccine development to second-generation mRNA technology
COVID-19 | Life Science History | Vaccine

CureVac shifted focus of COVID-19 vaccine development to second-generation mRNA technology

On Oct. 12, 2021, CureVac announced the strategic decision to focus its COVID-19 vaccine development towards the development…

Read More CureVac shifted focus of COVID-19 vaccine development to second-generation mRNA technologyContinue

Moderna announced COVAX exercised option to purchase 176.5 million additional doses of Moderna’s COVID-19 vaccine
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Moderna announced COVAX exercised option to purchase 176.5 million additional doses of Moderna’s COVID-19 vaccine

On Oct. 12, 2021, Moderna announced that Gavi, the Vaccine Alliance had exercised its option to purchase an…

Read More Moderna announced COVAX exercised option to purchase 176.5 million additional doses of Moderna’s COVID-19 vaccineContinue

INOVIO announced preprint publication of homologous boosting data for its COVID-19 DNA vaccine candidate  INO-4800
Biotechnology | COVID-19 | Infectious Disease | Vaccine

INOVIO announced preprint publication of homologous boosting data for its COVID-19 DNA vaccine candidate INO-4800

On Oct. 12, 2021, Inovio Pharmaceuticals announced online preprint publication in MedRxiv of Phase 1 clinical data on…

Read More INOVIO announced preprint publication of homologous boosting data for its COVID-19 DNA vaccine candidate INO-4800Continue

Resilience collaborated with Children’s Hospital of Philadelphia to develop next-gen biomanufacturing technologies
COVID-19 | Disease | HIV | Measles | Medicine | Pharmaceutical | Therapeutics | Vaccine

Resilience collaborated with Children’s Hospital of Philadelphia to develop next-gen biomanufacturing technologies

On Oct. 12, 2021, National Resilience announced a strategic collaboration with Children’s Hospital of Philadelphia (CHOP) to implement…

Read More Resilience collaborated with Children’s Hospital of Philadelphia to develop next-gen biomanufacturing technologiesContinue

Merck and Ridgeback announced Submission of EUA to the FDA for Molnupiravir, an Investigational Oral antiviral medicine, for treatment of COVID-19
COVID-19 | FDA | Life Science History

Merck and Ridgeback announced Submission of EUA to the FDA for Molnupiravir, an Investigational Oral antiviral medicine, for treatment of COVID-19

On Oct. 11, 2021, Merck and Ridgeback Biotherapeutics announced that Merck had submitted an Emergency Use Authorization (EUA)…

Read More Merck and Ridgeback announced Submission of EUA to the FDA for Molnupiravir, an Investigational Oral antiviral medicine, for treatment of COVID-19Continue

Washington University School of Medicine reported antiviral compound blocked SARS-CoV-2 from entering cells
Biotechnology | COVID-19 | Therapeutics

Washington University School of Medicine reported antiviral compound blocked SARS-CoV-2 from entering cells

On Oct. 11, 2021, scientists at Washington University School of Medicine in St. Louis announced they had developed…

Read More Washington University School of Medicine reported antiviral compound blocked SARS-CoV-2 from entering cellsContinue

INOVIO expanded INNOVATE phase 3 for INO-4800 to include Colombia
Biotechnology | COVID-19 | Infectious Disease | Vaccine

INOVIO expanded INNOVATE phase 3 for INO-4800 to include Colombia

On Oct. 11, 2021, Inovio Pharmaceuticals announced that it had received authorization from Colombia’s INVIMA, to conduct the…

Read More INOVIO expanded INNOVATE phase 3 for INO-4800 to include ColombiaContinue

Ebola case reported in the Democratic Republic of the Congo
Disease | WHO

Ebola case reported in the Democratic Republic of the Congo

On Oct. 8, 2021, the Ministry of Health of the Democratic Republic of the Congo announced that a…

Read More Ebola case reported in the Democratic Republic of the CongoContinue

PerkinElmer received FDA Emergency Use Authorization for respiratory SARS-CoV-2 panel
Biotechnology | COVID-19 | FDA | Infectious Disease | Influenza | Therapeutics

PerkinElmer received FDA Emergency Use Authorization for respiratory SARS-CoV-2 panel

On Oct. 7, 2021, PerkinElmer announced that the U.S. Food and Drug Administration (FDA) had issued Emergency Use…

Read More PerkinElmer received FDA Emergency Use Authorization for respiratory SARS-CoV-2 panelContinue

Duke University-led study showed Vaxart’s oral COVID-19 vaccine candidate reduced transmission of SARS-CoV-2 infection
Biotechnology | COVID-19 | Infectious Disease | Influenza | Vaccine

Duke University-led study showed Vaxart’s oral COVID-19 vaccine candidate reduced transmission of SARS-CoV-2 infection

On Oct. 7, 2021, Vaxart announced that a Duke University-led study published in bioRxiv showed that Vaxart’s (investigational…

Read More Duke University-led study showed Vaxart’s oral COVID-19 vaccine candidate reduced transmission of SARS-CoV-2 infectionContinue

Moderna announced state-of-the-art mRNA facility in Africa to manufacture up to 500 million doses per year
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Moderna announced state-of-the-art mRNA facility in Africa to manufacture up to 500 million doses per year

On Oct. 7, 2021, Moderna announced it was building a state-of-the-art mRNA facility in Africa with the goal…

Read More Moderna announced state-of-the-art mRNA facility in Africa to manufacture up to 500 million doses per yearContinue

BD unveiled Nebraska-based manufacturing capacity to support U.S. vaccination agility and preparedness
Diagnostics | NIH | Vaccine

BD unveiled Nebraska-based manufacturing capacity to support U.S. vaccination agility and preparedness

On Oct. 7, 2021, BD (Becton, Dickinson) announced it had strengthened the U.S. government’s access to safety injection…

Read More BD unveiled Nebraska-based manufacturing capacity to support U.S. vaccination agility and preparednessContinue

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